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FDA's End-of-Year Gifts: COVID-19 Diagnostic Tests and Collection Devices for Home Use | Morgan Lewis

To embed, copy and paste the code into your website or blog: The Food and Drug Administration (FDA or the Agency) spent the remaining weeks of 2020 issuing Emergency Use Authorizations (EUAs) for the first over-the-counter (OTC) COVID-19 test to be performed at home and the first OTC home sample collection kit for COVID-19 testing, as well as additional prescription at-home tests and sample collection kits. These newly authorized testing options are expected to help address the critical public ...
United States Morgan Lewis Clinical Laboratory Improvement Amendments Drug Administration Emergency Use Authorizations Home Test

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